Stereoselective total synthesis of both (6R,9R,10S,7E)- and (6S,9R,10S,7E)-epimers of oxylipin (9R,10S,7E)-6,9,10-trihydroxyoctadec-7-enoic acid

Tetrahedron

Volumn 69, Issue 9, 2013, Pages 2157-2166

  Saikia, Bishwajit ^a   Devi, Thongam Joymati ^a   Barua, Nabin C ^a  

^a CSIR NORTH EAST INSTITUTE OF SCIENCE AND TECHNOLOGY   (India)

Author keywords

Asymmetric synthesis; Dracontium loretense; Epimer; Immunostimulant; Oxylipin; PBMC

Indexed keywords

6,9,10 TRIHYDROXYOCTADEC 7 ENOIC ACID; BUTANOL; DRACONTIUM LORETENSE EXTRACT; EPOXIDE; OXYLIPIN; PLANT EXTRACT; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DRACONTIUM LORETENSE; DRUG ACTIVITY; DRUG SYNTHESIS; EPIMER; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; INFRARED SPECTROSCOPY; OLEFINATION; PRIORITY JOURNAL; PROTON NUCLEAR MAGNETIC RESONANCE; RING OPENING; STEREOCHEMISTRY; STEREOISOMERISM; WITTIG REACTION;

DRACONTIUM LORETENSE;

EID: 84873318775     PISSN: 00404020     EISSN: 14645416     Source Type: Journal    
DOI: 10.1016/j.tet.2012.12.076     Document Type: Article

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